Get Free Checker

How To Use Succinic acid In A Sentence

  • Aminoacidopathies (maple syrup urine disease; homocystinuria; cobalamin deficiencies; tyrosinemia; urea cycle defects (ornithine transcarbamylase, carbamyl phosphate synthase, citrullinemia, argininosuccinic aciduria, arginase deficiencies) and non-ketotic hyperglycinemia) Biochemical Genetics-Metabolic Disease
  • Aminoacidopathies (maple syrup urine disease; homocystinuria; cobalamin deficiencies; tyrosinemia; urea cycle defects (ornithine transcarbamylase, carbamyl phosphate synthase, citrullinemia, argininosuccinic aciduria, arginase deficiencies) and non-ketotic hyperglycinemia) Biochemical Genetics-Metabolic Disease
  • These acids transfer the system into the order: oxalacetic acid, malic acid, fumaric acid, and succinic acid, then, in the form of active hydrogen, to encounter the active oxygen from «the red system» and form water and free energy - a series of providentially subdued explosions which I alluded to before as a dramatic encounter. Physiology or Medicine 1937 - Presentation Speech
  • Aminoacidopathies (maple syrup urine disease; homocystinuria; cobalamin deficiencies; tyrosinemia; urea cycle defects (ornithine transcarbamylase, carbamyl phosphate synthase, citrullinemia, argininosuccinic aciduria, arginase deficiencies) and non-ketotic hyperglycinemia) Biochemical Genetics-Metabolic Disease
  • Treatment may include the use of chelating agents such as dimercaprol, dimercaptosuccinic acid, and dimercaptopanesulfonic acid.
Master English with Ease
Translate words instantly and build your vocabulary every day.
Boost Your
Learning
Master English with Ease
  • Chemet® (succimer) contains the stable meso isomer of dimercaptosuccinic acid which has also been known as DMSA. Succimer
  • The usual chemical process involves making succinic acid from crude oil or natural gas.
  • Aminoacidopathies (maple syrup urine disease; homocystinuria; cobalamin deficiencies; tyrosinemia; urea cycle defects (ornithine transcarbamylase, carbamyl phosphate synthase, citrullinemia, argininosuccinic aciduria, arginase deficiencies) and non-ketotic hyperglycinemia) Biochemical Genetics-Metabolic Disease
  • Polyepoxysuccinic acid ( PESA ) a new kind of biodegradable inhibitor.
  • Aminoacidopathies (maple syrup urine disease; homocystinuria; cobalamin deficiencies; tyrosinemia; urea cycle defects (ornithine transcarbamylase, carbamyl phosphate synthase, citrullinemia, argininosuccinic aciduria, arginase deficiencies) and non-ketotic hyperglycinemia) Biochemical Genetics-Metabolic Disease

Report a problem

Please indicate a type of error

Additional information (optional):